Diagnostic value of muscle MRI in differentiating LGMD2I from other LGMDs (Q57390205)

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article published in 2005

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Language	Label	Description	Also known as
English	Diagnostic value of muscle MRI in differentiating LGMD2I from other LGMDs	article published in 2005

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instance of

scholarly article

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title

Diagnostic value of muscle MRI in differentiating LGMD2I from other LGMDs (English)

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main subject

diagnosis

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magnetic resonance imaging

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author

Vincenzo Nigro

object named as

V. Nigro

series ordinal

6

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Hanns Lochmüller

object named as

H. Lochmüller

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9

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author name string

D. Fischer

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1

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M. C. Walter

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2

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K. Kesper

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3

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J. A. Petersen

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4

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S. Aurino

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5

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C. Kubisch

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7

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T. Meindl

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8

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K. Wilhelm

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10

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H. Urbach

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11

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R. Schröder

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12

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publication date

23 February 2005

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published in

Journal of Neurology

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volume

252

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issue

5

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page(s)

538-547

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cites work

Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophy.

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS00415-005-0684-4

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21 January 2018

Loss of calpain-3 autocatalytic activity in LGMD2A patients with normal protein expression.

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Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS00415-005-0684-4

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21 January 2018

A short protocol for muscle MRI in children with muscular dystrophies.

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS00415-005-0684-4

retrieved

21 January 2018

The phenotype of limb-girdle muscular dystrophy type 2I

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS00415-005-0684-4

retrieved

21 January 2018

Sarcolemmal proteins and the spectrum of limb-girdle muscular dystrophies

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15726252

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15726252

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Miyoshi-type distal muscular dystrophy. Clinical spectrum in 24 Dutch patients

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15726252

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Distal anterior compartment myopathy: a dysferlin mutation causing a new muscular dystrophy phenotype

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15726252

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s)

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15726252

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15726252

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On symptomatic heterozygous alpha-sarcoglycan gene mutation carriers

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15726252

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotypic spectrum associated with mutations in the fukutin-related protein gene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15726252

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15726252

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Consequences of a novel caveolin-3 mutation in a large German family

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15726252

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Magnetic resonance imaging of primary skeletal muscle diseases: patterns of distribution and severity of involvement

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15726252

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Duchenne muscular dystrophy: MR grading system with functional correlation

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15726252

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FKRP (826C>A) frequently causes limb-girdle muscular dystrophy in German patients

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15726252

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dysferlinopathy (LGMD2B): a 23-year follow-up study of 10 patients homozygous for the same frameshifting dysferlin mutations.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15726252

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Miyoshi myopathy in Saudi Arabia: clinical, electrophysiological, histopathological and radiological features

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15726252

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15726252

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variable reduction of caveolin-3 in patients with LGMD2B/MM.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15726252

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and imaging findings in six cases of congenital muscular dystrophy with rigid spine syndrome linked to chromosome 1p (RSMD1).

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15726252

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The phenotype of calpainopathy: diagnosis based on a multidisciplinary approach

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15726252

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Correlative MR imaging and 31P-MR spectroscopy study in sarcoglycan deficient limb girdle muscular dystrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15726252

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S00415-005-0684-4

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PubMed publication ID

15726252

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